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Major Depressive Disorder In The Elderly

This study is currently recruiting patients.

Sponsored by: GlaxoSmithKline
Information provided by: GlaxoSmithKline

Purpose

Placebo Controlled Study Evaluating the Effectiveness of Medication in Elderly Subjects with Major Depressive Disorder (MDD)

Condition Treatment or Intervention Phase
Major Depressive Disorder
 Drug: Investigational Major Depression Disorder drug
Phase III

MedlinePlus related topics:  Mental Health

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Eligibility

Ages Eligible for Study:  65 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

Exclusion Criteria:


Location and Contact Information


California
      Oceanside,  California,  92056,  United States; Recruiting
Study Coordinator  760-631-3056 

      Temecula,  California,  92591,  United States; Recruiting
Study Coordinator  880-670-4960 

Connecticut
      Norwich,  Connecticut,  06360,  United States; Recruiting
Study Coordinator  860-886-1508  Ext. 23 

Florida
      Miami,  Florida,  33125,  United States; Recruiting
Study Coordinator  305-321-6236 

      Miami,  Florida,  33125,  United States; Recruiting
Study Coordinator  305-642-3252 

      Ocala,  Florida,  34474,  United States; Terminated

Louisiana
      Shreveport,  Louisiana,  71101,  United States; Recruiting
Study Coordinator  318-227-4565 

Maryland
      Rockville,  Maryland,  20852,  United States; Terminated

New York
      New York,  New York,  10021,  United States; Recruiting
Study Coordinator  212-288-0138 

Pennsylvania
      Philadelphia,  Pennsylvania,  19149,  United States; Recruiting
Study Coordinator  215-624-1300 

Tennessee
      Memphis,  Tennessee,  38119,  United States; Recruiting
Study Coordinator  901-843-1045 

Texas
      Richardson,  Texas,  75080,  United States; Recruiting
Study Coordinator  972-907-1333 

More Information

Study ID Numbers:  AK130940
Record last reviewed:  October 2004
Record first received:  October 5, 2004
ClinicalTrials.gov Identifier:  NCT00093288
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2004-11-10
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